Inclusion body myositis – pathomechanism and lessons from genetics

Inclusion body myositis – pathomechanism and lessons from genetics

Inclusion body myositis is a rare, late-onset myopathy. Both inflammatory and myodegenerative features play an important role in their pathogenesis. Overlapping clinicopathological entities are the familial inclusion body myopathies with or without dementia. These myopathies share several clinical a...

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Bibliographic Details
Main Authors: Murnyák Balázs, Bodoki Levente, Vincze Melinda, Griger Zoltán, Csonka Tamás, Szepesi Rita, Kurucz Andrea, Dankó Katalin, Hortobágyi Tibor
Format: Article
Language:English
Published: De Gruyter 2015-02-01
Series:Open Medicine
Subjects:
sporadic inclusion body myositis
genetics
GNE
DES
VCP
IBMPFD
TDP-43
Online Access:http://www.degruyter.com/view/j/med.2015.10.issue-1/med-2015-0030/med-2015-0030.xml?format=INT

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http://www.degruyter.com/view/j/med.2015.10.issue-1/med-2015-0030/med-2015-0030.xml?format=INT

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